Warning letter
Herbalist and Alchemist, Inc.: warning letter of Sep 19, 2013
FDA warning letter 391185 · New Jersey District Office
Key facts
| Reference number | 391185 |
|---|---|
| Company | Herbalist and Alchemist, Inc. |
| Subject | CGMP/Dietary Supplement/Adulterated |
| Issue date | Sep 19, 2013 |
| Posted date | Sep 19, 2013 |
| Issuing office | New Jersey District Office |
| Product type | Food/Cosmetics |
| CFR sections cited | 111.75(a)(1)(ii), 111.75(c), 101, 101.36, 111, 111.70(b)(2), 111.70(e), 111.75(b), 101.36(c)(3), 101.36(e), 111.75(a)(1)(i), 111.75(a)(2) |
| Inspection city | Washington |
| Inspection ZIP | 07882 |
| Inspection start date | Oct 22, 2012 |
| Letter on fda.gov | web.archive.org |
At a glance
- 10–99 CFR sections cited
- OAI Linked inspection classification
- Yes Form FDA 483 issued
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA warning letters
FDA warning letters notify a firm of significant regulatory violations found during an inspection or review and request prompt corrective action.
Source: U.S. Food and Drug Administration (FDA), Warning Letters · Source date: